2021
DOI: 10.1016/j.foodchem.2020.128342
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Preparation and characterization of the encapsulated myrtle extract nanoliposome and nanoniosome without using cholesterol and toxic organic solvents: A comparative study

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Cited by 27 publications
(11 citation statements)
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“…Based on our research, only one study on myrtle extract in vesicle formulation was reported. Despite this, the extract was obtained from myrtle leaves [ 33 ]. In our study, liposomes were prepared by using a simple and fast method based on the sonication of phospholipids and the myrtle berry extract in the dispersant solution.…”
Section: Discussionmentioning
confidence: 99%
“…Based on our research, only one study on myrtle extract in vesicle formulation was reported. Despite this, the extract was obtained from myrtle leaves [ 33 ]. In our study, liposomes were prepared by using a simple and fast method based on the sonication of phospholipids and the myrtle berry extract in the dispersant solution.…”
Section: Discussionmentioning
confidence: 99%
“…Additionally, the polydispersity index (PdI) of lipid-based nanovesicles may affect their stability and is considered a key factor in particle size distribution. PdI values can range from 0 to 1.0 for an adequately monodisperse and polydisperse nanovesicle, respectively [ 20 ].…”
Section: Resultsmentioning
confidence: 99%
“…Zeta potential measurement is a common practice to determine the surface charge of colloidal systems, repulsion forces between them, and their physical stability [ 28 ]. Hence, the stability of nanoliposomes directly increases the increase in the repulsion of particles by either the electrostatic or steric repulsion of vesicles [ 20 ]. Acceptable zeta potential values to consider a system as stable range from lower than −30 mV to higher +30 mV [ 29 ] and are considered suitable for the colloidal stability of nanoliposomes [ 30 ].…”
Section: Resultsmentioning
confidence: 99%
“…The particle size of prepared liposomes was determined by a particle size analyzer (Zetasizer NanoZS 90, Malvern Company). The encapsulation efficiency (%) of C3G liposomes was measured by previous study to quantify the concentration of encapsulated C3G in the aqueous phase (Gorjian et al., 2021 ). A 2‐ml aliquot of the prepared liposome solution was collected and centrifuged by using a freeze centrifuge (Beckman) at 7104 g for 30 min at 4°C, and the total amount of C3G absorbance of each sample was recorded at 540 nm by a UV spectrophotometry(UV‐1200, China).…”
Section: Methodsmentioning
confidence: 99%